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水牛(Bubalus bubalis)精液在 Bioxcell 稀释液中的冷冻保存。

Cryopreservation of buffalo (Bubalus bubalis) semen in Bioxcell extender.

机构信息

Animal Physiology Laboratory, Department of Zoology, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi-46300, Pakistan.

出版信息

Theriogenology. 2010 Oct 1;74(6):951-5. doi: 10.1016/j.theriogenology.2010.04.024. Epub 2010 Jun 8.

Abstract

This study was designed to compare commercially available extender Bioxcell with tris-citric egg yolk extender for post thaw quality and in vivo fertility of buffalo semen. For comparison of post thaw semen quality: semen was collected from five adult Nili-Ravi buffalo (Bubalus bubalis) bulls of similar age group with artificial vagina (at 42 degrees C) for three weeks (replicates). Qualifying ejaculates having motility >60% from each buffalo bull were divided in two aliquots and diluted (at 37 degrees C having 50 x 10(6) spermatozoa/ml) in tris-citric egg yolk or Bioxcell extender. Diluted semen was cooled to 4 degrees C in 2 hours, equilibrated for 4 hours and filled in 0.5 ml straws. Semen straws were kept over liquid nitrogen vapors (5 cm) for 10 minutes. Straws were then plunged and stored in liquid nitrogen (-196 degrees C). After 24 hours of storage, semen straws were thawed at 37 degrees C for 30 seconds to assess sperm motility, viability, plasma membrane integrity, normal apical ridge, and abnormalities (head, mid piece, and tail). For comparison of in vivo fertility: semen from two buffalo bulls of known fertility was cryopreserved in tris-citric egg yolk and Bioxcell as described earlier, and used for inseminations under field conditions. Post-thaw percentage of sperm motility (45.3 +/- 1.1, 45.0 +/- 1.4), viability (66.2 +/- 1.1, 64.4 +/- 1.3) plasma membrane integrity (60.4 +/- 1.2, 59.2 +/- 1.4) and normal apical ridge (82.9 +/- 0.5, 80.7 +/- 0.5) did not differ (P > 0.05) in tris-citric egg yolk and Bioxcell extender, respectively. Similarly, sperm abnormalities of head (1.20 +/- 0.1, 1.20 +/- 0.1), mid piece (0.67 +/- 0.1, 0.87 +/- 0.1) and tail (11.7 +/- 0.2, 11.6 +/- 0.3) remained similar (P > 0.05) in tris-citric egg yolk and Bioxcell extender, respectively. In vivo fertility rates of buffalo semen cryopreserved in tris-citric egg yolk and Bioxcell also remained similar (44% vs. 47%). It is concluded that commercially available Bioxcell may be used for the cryopreservation of buffalo semen with an equal efficiency to tris-citric egg yolk extender.

摘要

本研究旨在比较市售的 extender Bioxcell 与 tris-citric 卵黄液 extender 在水牛精液解冻后质量和体内生育力方面的差异。为了比较解冻后精液质量:从五只成年 Nili-Ravi 水牛公牛(Bubalus bubalis)用人工阴道(在 42°C 下)收集了相似年龄组的精液(为期三周)(重复)。每个水牛公牛的活力>60%的合格精液被分为两份,并在 tris-citric 卵黄液或 Bioxcell 稀释液中稀释(在 37°C 下稀释至 50×10(6)个精子/ml)。稀释后的精液在 2 小时内冷却至 4°C,平衡 4 小时,然后装入 0.5 ml 细管中。精液细管在液氮蒸气(5cm)上保持 10 分钟。然后将细管浸入液氮中(-196°C)。在储存 24 小时后,将精液细管在 37°C 下解冻 30 秒,以评估精子活力、活力、质膜完整性、正常顶体嵴和异常(头部、中段和尾部)。为了比较体内生育力:已知生育力的两只水牛公牛的精液按照先前的描述在 tris-citric 卵黄液和 Bioxcell 中冷冻保存,并在田间条件下用于授精。解冻后精子活力(45.3+/-1.1、45.0+/-1.4)、活力(66.2+/-1.1、64.4+/-1.3)、质膜完整性(60.4+/-1.2、59.2+/-1.4)和正常顶体嵴(82.9+/-0.5、80.7+/-0.5)在 tris-citric 卵黄液和 Bioxcell 中的差异不显著(P>0.05)。同样,头部(1.20+/-0.1、1.20+/-0.1)、中段(0.67+/-0.1、0.87+/-0.1)和尾部(11.7+/-0.2、11.6+/-0.3)的精子异常在 tris-citric 卵黄液和 Bioxcell 中的差异也不显著(P>0.05)。在 tris-citric 卵黄液和 Bioxcell 中冷冻保存的水牛精液的体内生育力也相似(44%对 47%)。结论是,市售的 Bioxcell 可用于水牛精液的冷冻保存,其效率与 tris-citric 卵黄液 extender 相当。

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